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Guide

Understanding the latest IVDR Classification Rules

Discover our comprehensive guide to device classification rules for in-vitro diagnostic devices. Download your copy to ensure your products meet the requirements.

Guide

CE Marking Timeline in the UK Post-Brexit

Still confused about the timelines for CE Marking, EU MDR and the UKCA post Brexit? Our useful infographic should help.

Guide

Your free guide to current MDR Classification Rules

The classification of medical devices has changed with the implementation of the EU MDR. See how you’re affected in our handy infographic and complete guide.

Guide

The definitive guide to IFU for Medical Devices

We’ve collaborated with INSTRKTIV to share the definitive guide to IFU for medical devices and in-vitro diagnostic products. Discover all the requirements for both the US and EU markets.